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LeishmaniasisPhase 2NCT01300975

Intralesional Antimony for Bolivian Cutaneous Leishmaniasis

A Phase 2 study testing pentavalent antimony and cryotherapy in people with Leishmaniasis and Cutaneous Leishmaniasis, run by Fundacion Nacional de Dermatologia at 2 sites in Bolivia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Intralesional injection of antimony has been used for L major from Iran with a modest cure rate [56%: Asilian 2004]. However, this therapeutic approach has been used for L braziliensis from Brazil, with an attractive cure rate after 3 months of 80% [Oliveira-Neto 1997]. Read more about this study

Who is it for?
Ages 12 years and older
Conditions the study is for
Leishmaniasis, Cutaneous Leishmaniasis
What is being tested?
pentavalent antimony and cryotherapy
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
90 participants
Where
2 sitesBolivia
Study dates
Jan 2011to Jul 2012
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Gender: Male or female
  • Age: >12 yrs of age
  • Clinicla presentation: 1-2 ulcerative lesions, each < 30 mm in largest diameter, and with a total lesion area <900 mm2.
  • Parasitological confirmation of the lesion will be made by visualization or culture of leishmania from the biopsy or aspirate of the lesion.

Who cannot join

  • Previous treatment for leishmaniasis: therapy with Sb, pentamidine, amphotericin B, miltefosine, imidazoles or allopurinol in the last 3 months
  • Concomitant diseases by history that would be likely in the PI's opinion to interact, either positively or negatively, with IL Sb treatment.

Trial locations and contacts

2 sites in 1 country.

Bolivia2 sites
  • CUNETROP - Universidad Mayor de San Simon

    Cochabamba, CB

  • Hospital Dermatologico de Jorochito

    Jorochito, SC

Other trials in Bolivia

About this study

Official title: Short Course of Intralesional Antimony for Bolivian Cutaneous Leishmaniasis

Intralesional injection of antimony has been used for L major from Iran with a modest cure rate [56%: Asilian 2004]. However, this therapeutic approach has been used for L braziliensis from Brazil, with an attractive cure rate after 3 months of 80% [Oliveira-Neto 1997]. Because intralesional Sb injections is the local therapy with the best reported cure rate for South American L braziliensis disease, the species that causes disease in Bolivia, this pilot study of local therapy for bolivian L braziliensis disease will evaluate intralesional Sb therapy.

Read the detailed description

Cutaneous leishmaniasis is endemic in the New World from approximately the US-Mexican border through Central America and the Northern part of South America down to the level of Rio de Janeiro.

Until recently, the standard treatment for the leishmaniases was pentavalent antimony (Glucantime or Pentostam). The cure rate for L panamensis in Colombia is 91%-93% [Soto, 1993; Velez, 1997], a large study with several formulations of antimony found a combined Bolivia-Colombia cure rate of 86% [Soto, 2004b], and the cure rate in Palos Blancos, Bolivia is 15 of 16 = 94% [ Soto, 2008]. Nevertheless, pentavalent antimonials have the disadvantages of multiple injections during at least 3 weeks and mild-moderate clinical toxicity: local pain at the site of injections and generalized myalgias and arthralgias that can be severe and responsible for partial or definitive interruption of therapy, gastrointestinal complaints, liver enzyme elevations, pancreatic enzyme elevations and more rarely but with danger for life ventricular repolarization problems [Soto, 2005, Velez 2010], all of which are particularly unpleasant for a localized moderate clinical problem such as cutaneous leishmaniasis that usually is not dangerous for the patient.

The oral agent Miltefosine has now been shown to be as effective as antimony in Colombia and Bolivia. In Colombia, the cure rate for miltefosine was 91% [Soto 2004a] and in the just-completed trial in Palos Blancos, the cure rate for miltefosine was 32 of 37 = 88 % . Side effects seen in patients with cutaneous disease that can be specifically attributed to the drug are nausea and vomiting of mild grade in approximately 25% of patients, and low-grade elevation of creatinine also in approximately 25% of patients [Soto 2001; Soto 2004]. Now that cutaneous leishmaniasis is affecting more women at reproductive age, there is a crucial inconvenient because miltefosine can't be taken during pregnancy and breastfeeding; additionally prolonged courses (4 weeks) makes more difficult adherence to therapy and emerge the risk of incomplete treatments or it might be necessary supervised administration during the full course.

For small, single lesions, the side effects and cost of systemic therapy with antimony or miltefosine may outweigh the advantage of cure. For such lesions, targeted local therapy would be attractive if it is effective. The cost of goods will be low, and systemic adverse events would be non-existent.

For these reasons, topical treatment of the leishmaniases is presently the subject of intense worldwide interest, including at a recent [July 2010] PAHO meeting in Colombia. The leading candidates are topical formulations of paromomyin, local heat since cutaneous leishmania are heat-sensitive, local freezing as per any dermatologic lesion, and intralesional injections of antimony. The ability of topical formulations of paromomycin to cure depends on penetration of this divalent cation into the lesion and thus depends on the precise formula for the cream in which the paromomycin is dissolved. Other than the combination of paromomycin plus MBCL in Vaseline, which had minimal efficacy in Colombia [Soto 1998], patented paromomycin-containing creams are under investigation but cannot be obtained except from Pharma. Reports of local thermotherapy have been published, but again the key issue is penetration of the agent [in this case, heat] to the lesion and the best approach is difficult to utilize because it requires a $25,000 machine and exists a risk of infections via electrodes.

Intralesional injection of antimony has also been used for L major from Iran, and also with a modest cure rate [56%: Asilian 2004]. However, this therapeutic approach has been used for L braziliensis from Brazil, with an attractive cure rate after 3 months of 80% [Oliveira-Neto 1997]. Because intralesional Sb injections is the local therapy with the best reported cure rate for South American L braziliensis disease, the species that causes disease in Bolivia, this pilot study of local therapy for bolivian L braziliensis disease will evaluate intralesional Sb therapy.

Cryotherapy has been used as sole therapy for L major from Iran. The cure rate was modest: 50-60% [Asilian 2004; Layegh 2009]. Nevertheless, cryotherapy may have an attractive cure rate against L braziliensis. Therefore, cryotherapy will also be evaluated in this pilot study.

Patients receiving intralesional Sb will be randomized vs vs patients receiving cryotherapy and also vs patients receiving an emollient cream Because Il Sb has perhaps more promise than cryotherapy, more patients will receive Il Sb (30) than will receive cryotherapy (20) The emollient cream may improve host response to the trauma of the parasitic process, nevertheless, emollient cream is a placebo treatment in the specifically antiparasitic sense. The spontaneous rate of cure is unknown in Bolivia, thus this group will serve to establish this key value and permit comparison of the IL Sb rate and the cryotherapy rate to it. Although 20 patients will be randomized to the "placebo" group, stopping rules are such that if 4 early patients or 6 total patients in this group fail, no further "placebo" patients will be entered into the trial.

Being tested
pentavalent antimony, cryotherapy, placebo cream
Keywords
Leishmaniasis, intralesional antimony, cryotherapy
Medical subject headings
Leishmaniasis, Leishmaniasis, Cutaneous

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • pentavalent antimonyDrug

    3 intralesional injections of antimony at D1, D3 and D7

  • cryotherapyProcedure or surgery

    Frozing of lesions with liquid nitrogen ad D1 and D14

  • placebo creamDrug

    topical emollient crean 3 times a day during 21 days

Study groups in NCT01300975
Study groupRoleWhat they receive
Intralesional antimonyExperimental3 intralesional injections of antimony at D1, D3 and D7
Receives: Drug: pentavalent antimony
CryotherapyActive comparatorLiquid nitrogen until freezing at DF1 and D14
Receives: Procedure: cryotherapy
Topical creamPlacebo comparatortopical treatment 3 times a day during 21 days with an emollient cream
Receives: Drug: placebo cream

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Complete clinical cure

    100% epithelization, complete resolution of swelling and infiltration

    Measured: six months

Secondary outcomes (1)
  1. EKG changes associated with IL Sb, local reactions to cream and Cryo

    Ealuation of clinical findings and changes in OKG, lipase and SGOT in patients receiving intralesional antimony

    Measured: six months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Feb 2011 (estimated)
  2. Study startJan 2011
  3. Primary completionJul 2012
  4. Study completionJul 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
90 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01300975
Sponsor's protocol ID
ABF-BO-2010-101
Status last verified
Jul 2018
First submitted
17 Feb 2011
Last updated
2 Feb 2021
Results posted
No
Data monitoring committee
No

Publications

  • Chaabane H, Masmoudi A, Dammak A, Kchaou W, Akrout F, Zribi M, Boudaya S, Turki H. [Cryotherapy with or without intralesional antimony in the treatment of cutaneous leishmaniasis]. Ann Dermatol Venereol. 2009 Mar;136(3):278-9. doi: 10.1016/j.annder.2008.09.016. Epub 2008 Dec 3. No abstract available. French.

    PubMed 19328314
  • Ranawaka RR, Weerakoon HS. Randomized, double-blind, comparative clinical trial on the efficacy and safety of intralesional sodium stibogluconate and intralesional 7% hypertonic sodium chloride against cutaneous leishmaniasis caused by L. donovani. J Dermatolog Treat. 2010 Sep;21(5):286-93. doi: 10.3109/09546630903287445.

    PubMed 20438389
  • Soto J, Rojas E, Guzman M, Verduguez A, Nena W, Maldonado M, Cruz M, Gracia L, Villarroel D, Alavi I, Toledo J, Berman J. Intralesional antimony for single lesions of bolivian cutaneous leishmaniasis. Clin Infect Dis. 2013 May;56(9):1255-60. doi: 10.1093/cid/cit049. Epub 2013 Feb 6.

    PubMed 23390069

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing pentavalent antimony and cryotherapy in people with Leishmaniasis and Cutaneous Leishmaniasis, run by Fundacion Nacional de Dermatologia at 2 sites in Bolivia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Feb 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Bolivia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Complete clinical cure (time frame: six months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01300975, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2021.

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